Your browser doesn't support javascript.
loading
Detection of genome-wide low-frequency mutations with Paired-End and Complementary Consensus Sequencing (PECC-Seq) revealed end-repair-derived artifacts as residual errors.
You, Xinyue; Thiruppathi, Suresh; Liu, Weiying; Cao, Yiyi; Naito, Mikihiko; Furihata, Chie; Honma, Masamitsu; Luan, Yang; Suzuki, Takayoshi.
Afiliação
  • You X; School of Public Health, Hongqiao International Institute of Medicine, Shanghai Jiao Tong University School of Medicine, 227 South Chongqing Road, Shanghai, 200025, China.
  • Thiruppathi S; Division of Molecular Target and Gene Therapy Products, National Institute of Health Sciences, 3-25-26, Tonomachi, Kawasaki, 210-9501, Japan.
  • Liu W; Division of Molecular Target and Gene Therapy Products, National Institute of Health Sciences, 3-25-26, Tonomachi, Kawasaki, 210-9501, Japan.
  • Cao Y; School of Public Health, Hongqiao International Institute of Medicine, Shanghai Jiao Tong University School of Medicine, 227 South Chongqing Road, Shanghai, 200025, China.
  • Naito M; School of Public Health, Hongqiao International Institute of Medicine, Shanghai Jiao Tong University School of Medicine, 227 South Chongqing Road, Shanghai, 200025, China.
  • Furihata C; Division of Genetics and Mutagenesis, National Institute of Health Sciences, 3-25-26, Tonomachi, Kawasaki, 210-9501, Japan.
  • Honma M; Division of Molecular Target and Gene Therapy Products, National Institute of Health Sciences, 3-25-26, Tonomachi, Kawasaki, 210-9501, Japan.
  • Luan Y; Division of Molecular Target and Gene Therapy Products, National Institute of Health Sciences, 3-25-26, Tonomachi, Kawasaki, 210-9501, Japan.
  • Suzuki T; Division of Genetics and Mutagenesis, National Institute of Health Sciences, 3-25-26, Tonomachi, Kawasaki, 210-9501, Japan.
Arch Toxicol ; 94(10): 3475-3485, 2020 10.
Article em En | MEDLINE | ID: mdl-32737516
Assuntos
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Análise Mutacional de DNA / Sequenciamento de Nucleotídeos em Larga Escala / Taxa de Mutação Idioma: En Ano de publicação: 2020 Tipo de documento: Article País de afiliação: China
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Análise Mutacional de DNA / Sequenciamento de Nucleotídeos em Larga Escala / Taxa de Mutação Idioma: En Ano de publicação: 2020 Tipo de documento: Article País de afiliação: China